Zobrazeno 1 - 10
of 53
pro vyhledávání: '"V V Rameev"'
Autor:
L V Kozlovskaya, V V Rameev, T V Androsova, I N Kogarko, B S Kogarko, N N Mrykhin, I G Rekhtina
Publikováno v:
Терапевтический архив, Vol 88, Iss 12, Pp 82-87 (2016)
The article deals with the so-called monoclonal gammopathy of undetermined significance (MGUS), which is being actively explored in the world and has been recently investigated in Russia. It indicates the principles of identifying the phenotypes of M
Externí odkaz:
https://doaj.org/article/456fd0bd76a54e07bd3394202e26933d
Publikováno v:
Терапевтический архив, Vol 88, Iss 6, Pp 58-64 (2016)
Aim. To determine the possibility of using the serum proinflammatory calcium-binding protein, or calgranulin C (S100A12), to assess activity and therapeutic efficiency in patients with periodic disease (PD) and other familial periodic fevers (FPFs).
Externí odkaz:
https://doaj.org/article/3f68db3201fe477db2d6e9b2996fa2f3
Publikováno v:
Терапевтический архив, Vol 87, Iss 6, Pp 108-111 (2015)
It is currently well justified that monoclonal gammopathies are the most important predictor for kidney diseases, including glomerulonephritis. To determine a correlation of nephropathy with oligosecretory gammopathy is of fundamental importance, as
Externí odkaz:
https://doaj.org/article/dafa1f82e98448d9bfbf58fbd16fafd6
Publikováno v:
Терапевтический архив, Vol 85, Iss 6, Pp 51-59 (2013)
The paper gives current general data on the structure of amyloid fibril and the principles in the classification of amyloidosis, information on the clinical course of cardiac and renal involvements in systemic AL and AA amyloidosis, and that on diagn
Externí odkaz:
https://doaj.org/article/3faaecdc660a4eed8735ef7853d7d3e6
Publikováno v:
Терапевтический архив, Vol 84, Iss 6, Pp 53-59 (2012)
A significant progress in the field of molecular-biological investigations resulted in definition of a new group of systemic diseases referred to as autoinflammatory. This group comprises familial periodic fevers: periodic disease (mediterranean feve
Externí odkaz:
https://doaj.org/article/597bfc3aa2204a7a91b4b4da39dd7955
Autor:
Vilen Vilevich Rameev, Lidiya Vladimirovna Kozlovskaya, Elena Aleksandrovna Malinina, Anna Grigor'evna Serova, Ivetta Nikolaevna Kogarko, Bronislav Stanislavovich Kogarko, Nina Vasil'evna Lyubimova, V V Rameev, L V Kozlovskaya, E A Malinina, A G Serova, I N Kogarko, B S Kogarko, N V Lyubimova
Publikováno v:
Терапевтический архив, Vol 83, Iss 8, Pp 48-54 (2011)
Aim. To determine clinical significance of measuring blood levels of protein precursors of AA- and AL-amyloidosis - SAA and immunoglobulin free light chains (ILC), respectively. Material and methods. SAA concentrations were studied with ELISA in 43 r
Externí odkaz:
https://doaj.org/article/5821d029259d43a2bdbeadbe21c17514
Autor:
Mayra Latypovna Nanchikeeva, Lidiya Vladimirovna Kozlovskaya, Vilen Vilevich Rameev, Viktor Viktorovich Fomin, Nikolay Mikhaylovich Bulanov, M L Nanchikeeva, L V Kozlovskaya, V V Rameev, V V Fomin, N M Bulanov
Publikováno v:
Терапевтический архив, Vol 83, Iss 6, Pp 23-27 (2011)
Aim. To determine clinical significance of urinary biomarkers of proteolysis/fibrinolysis and fibroangiogenesis in essential hypertension (EH). Material and methods. Examination of the kidneys was made in 71 patients with EH degree 1-3. Renal functio
Externí odkaz:
https://doaj.org/article/e95dfa893aa74a559e952d8e147c5042
Autor:
Viktor Viktorovich Fomin, V V Rameev, V P Sedov, M M Severova, A V Svet, N G Miroshnichenko, L V Kozlovskaya, V V Fomin, V V Rameyev
Publikováno v:
Терапевтический архив, Vol 0, Iss 1, Pp 73-77 (2010)
The paper describes a clinical case of congenital cardiomyopathy (left ventricular noncompaction) concurrent with secondary amyloidosis and renal involvement that develops at the outcome of long existing brochoectatic disease.
Externí odkaz:
https://doaj.org/article/8e0d774c8d4f4488a11a75f4c3d6f86f
Autor:
S. O. Salugina, A. V. Torgashina, E. Yu. Borzova, V. V. Rameev, V. R. Gorodetskiy, E. S. Fedorov, N. V. Muravyeva
Publikováno v:
Научно-практическая ревматология, Vol 61, Iss 6, Pp 711-722 (2024)
The aim – to present the experience of diagnosis, management, and therapy with IL-1 inhibitors in patients with Schnitzler’s syndrome (SchS) according to a multicenter Russian cohort.Materials and methods. In an observational retrospective study
Externí odkaz:
https://doaj.org/article/3ef03064569c46a69d9d20a51383e7e4
Autor:
E. I. Safiulina, O. E. Zinovieva, N. S. Shcheglova, V. V. Rameev, Z. V. Surnina, E. N. Nikitina, O. A. Vorobieva
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 14, Iss 6, Pp 67-72 (2022)
Hereditary transthyretin amyloidosis belongs to a group of diseases with an autosomal dominant type of transmission and a heterogeneous clinical picture, which depends on the type of transthyretin gene mutation. The leptomeningeal form is a rare phen
Externí odkaz:
https://doaj.org/article/7d08b9bd50d84effb6057a28fa24dce7